TUBING, DIALYSATE (AND CONNECTOR)
K-Number: K022068 · 2002-09-23
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Device Summary
Frequently Asked Questions
What is the TUBING, DIALYSATE (AND CONNECTOR)?
TUBING, DIALYSATE (AND CONNECTOR) is a medical device that received FDA 510(k) clearance on 2002-09-23. The listed applicant is Molded Products, Inc.. The 510(k) number is K022068.
When did TUBING, DIALYSATE (AND CONNECTOR) receive FDA 510(k) clearance?
TUBING, DIALYSATE (AND CONNECTOR) received FDA 510(k) clearance on 2002-09-23, under 510(k) number K022068.
Who is the listed applicant for TUBING, DIALYSATE (AND CONNECTOR)?
The FDA 510(k) record lists Molded Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBING, DIALYSATE (AND CONNECTOR)?
The FDA product code for TUBING, DIALYSATE (AND CONNECTOR) is FID.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Molded Products, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FID)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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